Fijiana Kkava Dealers
⚠️ Moderate Risk
FEI: 3004424885 • Suva • FIJI
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
How is this score calculated?
Proprietary Algorithm
- 40% Violation Severity — AI-assessed (1-10)
- 30% Refusal Volume — Logarithmic scale
- 20% Recency — Decays over 5 years
- 10% Frequency — Refusals per year
© ImportRefusal.com Original Analysis
Violation Summary
PESTICIDES
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be adulterated because it contains a pesticide chemical, which is in violation of section 402(a)(2)(B). Contains:
Refusal History
Frequently Asked Questions
What is Fijiana Kkava Dealers's FDA import refusal history?
Fijiana Kkava Dealers (FEI: 3004424885) has 2 FDA import refusal record(s) in our database, spanning from 4/8/2008 to 11/4/2008.
What is an FEI number?
FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Fijiana Kkava Dealers's FEI number is 3004424885.
What types of violations has Fijiana Kkava Dealers received?
Fijiana Kkava Dealers has been cited for 1 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.
Where does this information about Fijiana Kkava Dealers come from?
All FDA import refusal data for Fijiana Kkava Dealers is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.
Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.